Newsletter May 2018
- China: successful CMEF and seminar for consulting companies
- Ukraine: MEDCERT Cooperation with IMPROVE MEDICAL LLC
- EU: MDCG – The European Commission published its first guidance documents on the MDR
- Canada: Updated guidance on classification for “Device” or “Drug“ products
- Canada: New Reclassification Rules for certain Device Disinfectants And Sterilants
- Malaysia: New Guidance on Labelling Requirements for Medical Devices
- Canada: Adjustments to the Medical Device Single Audit Program (MDSAP) Transition
- ATTENTION: fake MEDCERT certificates